Diels–Alder reactions of activated furans to cyclopentenone derivatives: a regiodivergent Diels–Alder approach towards polyfunctionalised cis-hydrindanones-Reference-Cited by-同舟云学术

Diels–Alder reactions of activated furans to cyclopentenone derivatives: a regiodivergent Diels–Alder approach towards polyfunctionalised cis-hydrindanones

Published:2000-08 Issue:33 Volume:41 Page:6377-6381
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Trembleau Laurent,Patiny Luc,Ghosez Léon

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

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3. This has been recently challenged by Ayyad et al. who have isolated ottelione A and its trans-fused stereoisomer ottelione B from Ottelia alismoides originating from the Nile Delta. These authors claim to have established the relative configuration of the benzyl and vinyl groups to be cis on the basis of NMR studies: Ayyad, S. E. N.; Judd, A. S.; Shier, W. T.; Hoye, T. R. J. Org. Chem. 1998, 63, 8102.

4. Mehta, G.; Reddy, D. S. Chem. Commun. 1999, 2193.

5. For a recent review on synthetic applications of furan Diels–Alder chemistry: Kappe, C. O.; Murphree, S. S.; Padwa, A. Tetrahedron 1997, 53, 14179.

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